In assisted reproductive technology (ART), Urofollitropin—a highly purified
urinary follicle-stimulating hormone (FSH)—is a cornerstone of ovulation
induction therapy, trusted for its proven efficacy and safety profile. As key
patents for recombinant FSH (the dominant ART hormone) approach expiration in
major markets by 2026, the global landscape is witnessing a shift toward
cost-effective alternatives, making Urofollitropin price a focal point for
clinics, distributors, and infertile couples. Navigating Urofollitropin price
dynamics while ensuring uncompromised efficacy has become a critical task for
stakeholders seeking to optimize ART treatment accessibility and
affordability.
Urofollitropin price is shaped by a unique interplay of production
complexity, market competition, and regional regulatory policies—distinct from
synthetic alternatives. As a urinary-derived hormone, Urofollitropin requires
rigorous purification processes to eliminate impurities, which influences its
pricing, though it remains 30-40% more cost-effective than recombinant FSH.
Post-patent market shifts are further impacting Urofollitropin price: with the
influx of recombinant FSH generics, Urofollitropin manufacturers are optimizing
production chains to maintain competitive pricing without sacrificing quality.
For example, in the European market, Urofollitropin price per 75 IU vial ranges
from $35 to $50, significantly lower than branded recombinant FSH at $80-$120,
while delivering comparable clinical outcomes.

The cost-efficacy of Urofollitropin, underscored by its stable price point,
makes it an ideal choice for resource-constrained clinics and patients requiring
multiple ART cycles. Clinical studies confirm that Urofollitropin achieves
similar pregnancy rates (42-45%) to recombinant FSH in patients with normal
ovarian reserve, while reducing per-cycle medication costs by approximately 35%.
This balance is particularly valuable in emerging markets, where ART
accessibility is limited by high treatment costs. Moreover, Urofollitropin price
stability—compared to volatile recombinant FSH pricing affected by patent
transitions—enables clinics to plan budgets reliably, enhancing treatment
accessibility for broader patient groups.
Kangyuan leverages advanced production technologies to optimize
Urofollitropin price while upholding strict global quality standards. Our
streamlined purification processes, combined with a traceable raw material
supply chain (sourced from healthy donors), reduce production costs without
compromising bioactivity. We offer flexible formulations (75 IU and 150 IU
vials) to align with personalized treatment plans, allowing clinics to minimize
waste and further control costs. Kangyuan’s Urofollitropin meets USP, EP, and
Chinese Pharmacopoeia standards, ensuring efficacy comparable to international
brands at a competitive price point, making it a trusted choice in both mature
and emerging ART markets.
As the ART market evolves post-patent, Urofollitropin price competitiveness
and proven efficacy position it as a sustainable solution for global
reproductive healthcare. Kangyuan remains committed to advancing accessible ART
by maintaining stable Urofollitropin pricing and uncompromising quality. Our
professional team provides tailored support to clinics and distributors,
including volume-based pricing options and technical guidance to optimize
treatment protocols. Whether you are a clinic seeking cost-effective ovulation
induction solutions, or a distributor expanding ART product portfolios, Kangyuan
is your reliable partner. Contact us today to explore our Urofollitropin product
range and unlock tailored solutions for your market needs.